Organo-Metalloid Compounds
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Filtered Search Results
Medchemexpress LLC Boc-NH-PEG3 | 139115-92-7 | MFCD07357496 | ≥98.0% | 249.30 | C11H23NO5 | 5 G
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Boc-NH-PEG3 is a polyethylene glycol-based linker bearing a Boc-protected amino group and a triethylene glycol spacer. It is intended as a synthetic building block for assembling bifunctional degraders and other conjugates, providing aqueous solubility and a protected amine for downstream coupling reactions.
- Boc-protected amine provides a protected functional handle for synthesis.
- Triethylene glycol spacer increases solubility and conformational flexibility.
- High purity suitable for chemical synthesis (≥98.0%).
- Multiple package sizes available to support small- and large-scale work.
- Storage recommendations extend shelf life when followed.
- Liquid, colorless to light yellow, convenient for handling and formulation.
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Aobchem Benzylboronic acid pinacol ester, AOBCHEM USA 10364-5G. 87100-28-5. MFCD05663841
Benzylboronic acid pinacol ester, AOBCHEM USA 10364-5G. 87100-28-5. MFCD05663841
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000405223 TRIMETHOXY 4-PHENYLB 100MG
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eMolecules TOS-PEG5 T-BUTYL ESTER 25G
5000193072 TOS-PEG5 T-BUTYL ESTER 25G
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eMolecules 4-TERT-BUTYLDIMETHYLSIL 25G
5000158865 4-TERT-BUTYLDIMETHYLSIL 25G
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eMolecules CYCLOPENT-2-ENONE 1G
5000158806 CYCLOPENT-2-ENONE 1G
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eMolecules 2-DICHLOROMETHYL-4 4 5 5- 5G
5000159107 2-DICHLOROMETHYL-4 4 5 5- 5G
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eMolecules 3 4-DIMETHOXY-3-CYCLOBUTENE 5G
5000159932 3 4-DIMETHOXY-3-CYCLOBUTENE 5G
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Selleck Chemical LLC PS-1145
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PS-1145 is a specific IKK inhibitor with IC50 of 88 nM
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Apexbio Technology LLC NVR 3-778 1445790-55-5 1mg
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NVR 3-778 (CAS 1445790-55-5) is a small-molecule modulator targeting the hepatitis B virus (HBV) core protein It is designed to interfere with HBV capsid assembly thereby inhibiting viral genome encapsidation and replication NVR 3-778 exerts its biological activity primarily by disrupting capsid formation and reducing viral replication In in vitro studies NVR 3-778 demonstrates antiviral inhibition with a half-maximal inhibitory concentration (IC50) reported in the low micromolar range Based on these pharmacological properties NVR 3-778 holds research potential in the investigation of HBV biology and the development of alternative therapeutic approaches for chronic hepatitis B infection
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Apexbio Technology LLC PS-1145 431898-65-6 5mg
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PS-1145 (CAS 431898-65-6) is a selective inhibitor of I B kinase (IKK) with an IC50 of 88 nM IKK is a critical component of the upstream NF- B signaling pathway regulating cellular responses to inflammation In vitro studies have demonstrated that PS-1145 blocks TNF -induced NF- B activation in multiple myeloma (MM) cells in a dose- and time-dependent manner increases I B protein levels suppresses IL-6-mediated anti-apoptotic effects and inhibits expression of ICAM-1 Additionally PS-1145 reduces IL-6 secretion from bone marrow stromal cells (BMSCs) and partially limits MM cell proliferation In vivo PS-1145 has been shown to induce apoptosis in DMBA-induced skin tumors in rats by inhibiting NF- B and VEGF activity The compound remains in the preclinical research stage
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eMolecules 3-BROMO-1 1-DIFLUORO-CYCLOB 5G
5000159276 3-BROMO-1 1-DIFLUORO-CYCLOB 5G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
5000434695 5-BROMO-2-TRIFLUOROM 10G
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eMolecules 4-(TERT-BUTYLDIMETHYLSILYLOXY) CYCLOHEXANAMINE | 121936-51-4 | MFCD18206131 | 1g
AstaTech | 4-(TERT-BUTYLDIMETHYLSILYLOXY) CYCLOHEXANAMINE | 1g | 273176308 | AB10752 | 95.000 | 121936-51-4 | MFCD18206131 | 229.439 | C12H27NOSi
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Medchemexpress LLC (S,R,S)-AHPC-C2-amide-benzofuranylmethyl-pyridine | 2347517-69-3 | 98.6% | C41H46N6O6S | 10MG
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(S,R,S)-AHPC-C2-amide-benzofuranylmethyl-pyridine is a PROTAC small-molecule research reagent that induces ubiquitination and degradation of Smad3 while modulating HIF-α protein levels. It is intended for preclinical studies of anti-fibrosis, renal protection, and oncology mechanisms and is supplied as a high-purity solid.
- High purity (98.6%) for reliable experimental results.
- Dual-target PROTAC mechanism induces Smad3 degradation and modulates HIF-α levels.
- Suitable for preclinical research in fibrosis, renal protection, and oncology.
- Supplied as a solid and available in small research pack sizes for screening and synthesis.
- High solubility in DMSO (≥170 mg/mL) for convenient stock preparation.
- Stable under recommended storage conditions to preserve activity.
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